[PDF][PDF] Interplay between cytosolic dopamine, calcium, and α-synuclein causes selective death of substantia nigra neurons

EV Mosharov, KE Larsen, E Kanter, KA Phillips… - Neuron, 2009 - cell.com
EV Mosharov, KE Larsen, E Kanter, KA Phillips, K Wilson, Y Schmitz, DE Krantz
Neuron, 2009cell.com
The basis for selective death of specific neuronal populations in neurodegenerative
diseases remains unclear. Parkinson's disease (PD) is a synucleinopathy characterized by a
preferential loss of dopaminergic neurons in the substantia nigra (SN), whereas neurons of
the ventral tegmental area (VTA) are spared. Using intracellular patch electrochemistry to
directly measure cytosolic dopamine (DA cyt) in cultured midbrain neurons, we confirm that
elevated DA cyt and its metabolites are neurotoxic and that genetic and pharmacological …
Summary
The basis for selective death of specific neuronal populations in neurodegenerative diseases remains unclear. Parkinson's disease (PD) is a synucleinopathy characterized by a preferential loss of dopaminergic neurons in the substantia nigra (SN), whereas neurons of the ventral tegmental area (VTA) are spared. Using intracellular patch electrochemistry to directly measure cytosolic dopamine (DAcyt) in cultured midbrain neurons, we confirm that elevated DAcyt and its metabolites are neurotoxic and that genetic and pharmacological interventions that decrease DAcyt provide neuroprotection. L-DOPA increased DAcyt in SN neurons to levels 2- to 3-fold higher than in VTA neurons, a response dependent on dihydropyridine-sensitive Ca2+ channels, resulting in greater susceptibility of SN neurons to L-DOPA-induced neurotoxicity. DAcyt was not altered by α-synuclein deletion, although dopaminergic neurons lacking α-synuclein were resistant to L-DOPA-induced cell death. Thus, an interaction between Ca2+, DAcyt, and α-synuclein may underlie the susceptibility of SN neurons in PD, suggesting multiple therapeutic targets.
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